Controlling ${}^{229}$Th isomeric state population in a VUV transparent crystal

Abstract

The radioisotope Th-229 is renowned for its extraordinarily low-energy, long-lived nuclear first-excited state. This isomeric state can be excited by VUV lasers and the transition from the ground state has been proposed as a reference transition for ultra-precise nuclear clocks. Such nuclear clocks will find multiple applications, ranging from fundamental physics studies to practical implementations. Recent investigations extracted valuable constraints on the nuclear transition energy and lifetime, populating the isomer in stochastic nuclear decay of U-233 or Ac-229. However, to assess the feasibility and performance of the (solid-state) nuclear clock concept, time-controlled excitation and depopulation of the ${}^{229}$Th isomer together with time-resolved monitoring of the radiative decay are imperative. Here we report the population of the ${}^{229}$Th isomeric state through resonant X-ray pumping and detection of the radiative decay in a VUV transparent ${}^{229}$Th-doped CaF${}_2$ crystal. The decay half-life is measured to $447\pm 25$ s, with a transition wavelength of $148.18\pm 0.42$ nm and a radiative decay fraction consistent with unity. Furthermore, we report a new ``X-ray quenching'' effect which allows to de-populate the isomer on demand and effectively reduce the half-life by at least a factor 50. Such controlled quenching can be used to significantly speed up the interrogation cycle in future nuclear clock schemes. Our results show that full control over the ${}^{229}$Th nuclear isomer population can be achieved in a crystal environment. In particular, non-radiative decay processes that might lead to a broadening of the isomer transition linewidth are negligible, paving the way for the development of a compact and robust solid-state nuclear clock. Further studies are needed to reveal the underlying physical mechanism of the X-ray quenching effect.

14 pages with 8 figures and 2 tables

References in corpus (8)

• Enhanced effect of temporal variation of the fine structure constant in diatomic molecules
• Observation of the radiative decay of the ${}^{229}\mathrm{Th}$ nuclear clock isomer
• Measurement of the ${}^{229}$Th isomer energy with a magnetic micro-calorimeter
• Performance of a 229 Thorium solid-state nuclear clock
• Energy of the ${}^{229}$Th Nuclear Clock Isomer Determined by Absolute $\gamma$-ray Energy Difference
• Optical Transmission Enhancement of Ionic Crystals via Superionic Fluoride Transfer: Growing VUV-Transparent Radioactive Crystals
• Nuclear coherent population transfer to the ${}^{229m}$Th isomer using x-ray pulses
• Estimation of radiative half-life of ${}^{229m}$Th by half-life measurement of other nuclear excited states in ${}^{229}$Th

Cited by in corpus (8)

• Frequency ratio of the ${}^{229\mathrm{m}}$Th nuclear isomeric transition and the ${}^{87}$Sr atomic clock
• ${}^{229}{\mathrm{ThF}}_4$ thin films for solid-state nuclear clocks
• Radiative Decay of the ${}^{229m}$Th Nuclear Clock Isomer in Different Host Materials
• A continuous-wave vacuum ultraviolet laser for the nuclear clock
• Quantum Sensing Using Atomic Clocks for Nuclear and Particle Physics
• A cryogenic Paul trap for probing the nuclear isomeric excited state ${}^{229\text{m}}$Th${}^{3+}$
• Constraints on the Variation of the QCD Interaction Scale ${\Lambda }_{\text{QCD}}$
• Theoretical evaluation of decay mode of ${}^{229m}\mathrm{Th}$ in solid samples